Limb-girdle muscular dystrophy-dystroglycanopathy, type C2

Common Name(s)

Limb-girdle muscular dystrophy-dystroglycanopathy, type C2

MDDGC2 is an autosomal recessive muscular dystrophy with onset after ambulation is achieved. Cognition is normal ({1:Biancheri et al., 2007}). It is part of a group of similar disorders resulting from defective glycosylation of DAG1, collectively known as 'dystroglycanopathies' ({2:Godfrey et al., 2007}). For a discussion of genetic heterogeneity of muscular dystrophy-dystroglycanopathy type C, see MDDGC1 ({609308}).
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Limb-girdle muscular dystrophy-dystroglycanopathy, type C2" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

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Scientific Literature

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Symptoms, Diagnosis, and Treatment

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